RSS Events Feeds

Medical Device QSR Compliant Product Development Process One and half day Inperson Seminar

1/23/2014 8:30 AM - 1/24/2014 1:30 PM

Learning Objectives:

The seminar will focus on understanding:

-The key elements of 21 CFR 820 design controls

-Best practice stage gate product development

-How 21 CFR 820 design controls can be integrated into a stage gate product development process

-How to link to intended use, user needs, risk management and manufacturing processes

-How to manage both new product development and design changes

-How to manage marketing, costs and schedule requirements in parallel with the regulatory processes

-How to systematically create the required objective evidence and how to easily produce it during an audit

Who will Benefit:

-Project managers

-Quality managers and staff

-R & D, product development and sustaining engineering, managers and staff

-Design transfer managers and staff

-Regulatory and compliance managers and staff

-Compliance and product development consultants

-Anyone with product development, risk management, regulator or quality assurance responsibilities

Learn More: Medical Device QSR Compliant Product Development Process One and half day Inperson Seminar

Events Map

Email Newsletters

Want to be up-to-date with the latest news and updates from Entrepreneurship.org? To subscribe, just give us your email address below; you'll choose which e-newsletters you'd like to receive on the next screen.